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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
muscular disease +     
Reperfusion Injury +     
arthrogryposis multiplex congenita +   
Axial Myopathy, Late-Onset +   
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
Carey-Fineman-Ziter syndrome +   
Chanarin-Dorfman syndrome +   
Chronic Allograft Dysfunction +   
chronic fatigue syndrome  
compartment syndrome +   
Congenital Myopathy with Neuropathy and Deafness  
Congenital Universal Muscular Hypoplasia of Krabbe 
Contracture +   
Craniomandibular Disorders +   
diaphragm disease +   
Dimauro Disease  
Ehlers-Danlos syndrome kyphoscoliotic type 2  
eosinophilia-myalgia syndrome  
Erythrocyte Amp Deaminase Deficiency  
Erythrocyte Lactate Transporter Defect  
familial periodic paralysis +   
fibromyalgia +   
Fingerprint Body Myopathy 
Gamstorp-Wohlfart syndrome  
Gastric Reperfusion Injury  
Granulovacuolar Lobular Myopathy with Electrical Myotonia 
Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis  
Hypertrophia Musculorum Vera 
Internal Anal Sphincter Myopathy 
Intestinal Reperfusion Injury  
Kidney Reperfusion Injury +   
Kocher-Debre-Semelaigne Syndrome 
Late-Onset Carnitine Palmitoyltransferase II Deficiency  
limb reperfusion injury  
Liver Reperfusion Injury  
Lung Reperfusion Injury +   
Marinesco-Sjogren syndrome  
Medial Tibial Stress Syndrome 
Mitochondrial DNA Depletion Syndrome, Myopathic Form +   
Muscle Cramp +   
Muscle Rigidity +   
Muscle Spasticity +   
muscle tissue disease +   
Muscle Weakness +   
Musculoskeletal Pain +   
Myalgia +   
Myocardial Reperfusion Injury  
myofascial pain syndrome +   
Myopathic Carnitine Deficiency 
Myopathy with Lactic Acidosis, Hereditary  
myotonic disease +   
Myotoxicity 
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria 
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy 
Ovary Reperfusion Injury  
Pectoralis Muscle, Absence of 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
Primary Graft Dysfunction  
Proximal Myopathy with Focal Depletion of Mitochondria 
Retina Reperfusion Injury  
Rhabdomyolysis +   
Singleton Merten Syndrome +   
Skeletal Muscle Injuries  
Skeletal Muscle Reperfusion Injury  
Adverse functional, metabolic, or structural changes in ischemic tissues resulting from the restoration of blood flow to skeletal muscle, including swelling; hemorrhage; necrosis; and damage from free radicals.
Spinal Cord Reperfusion Injury  
systemic primary carnitine deficiency disease  
Tel Hashomer Camptodactyly Syndrome 
tendinitis +   
Testis Reperfusion Injury  
transient cerebral ischemia +   
Treft Sanborn Carey Syndrome 
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
Urinary Bladder Reperfusion Injury  
Uruguay faciocardiomusculoskeletal syndrome  
Vacuolar Myopathy  
very long chain acyl-CoA dehydrogenase deficiency  

Synonyms
Primary IDs: RDO:9000692

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